Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 1,021

The DOI matches its Crossref record; 301 of the 301 references it cites were found in a registry or an index.

Therapeutic strategies for enhancing angiogenesis in wound healing

Open access
Veith, Austin P., Henderson, Kayla, Spencer, Adrianne, Sligar, Andrew D., Baker, Aaron B.·2019·Advanced Drug Delivery Reviews
DOI 10.1016/j.addr.2018.09.010
Open this paper in CoChat — free account

Abstract

The enhancement of wound healing has been a goal of medical practitioners for thousands of years. The development of chronic, non-healing wounds is a persistent medical problem that drives patient morbidity and increases healthcare costs. A key aspect of many non-healing wounds is the reduced presence of vessel growth through the process of angiogenesis. This review surveys the creation of new treatments for healing cutaneous wounds through therapeutic angiogenesis. In particular, we discuss the challenges and advancement that have been made in delivering biologic, pharmaceutical and cell-based therapies as enhancers of wound vascularity and healing.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.addr.2018.09.010

Cites

301 of 301 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

1 retracted

Show all 301 references

Research works printed but not linked: 36

  1. Park, 2013, Updating on understanding and managing chronic wound, Dermatol Ther, 26, 236, 10.1111/dth.12052 · doi:10.1111/dth.12052
  2. Ayello, 2005, What does the wound say? Why determining etiology is essential for appropriate wound care, Adv Skin Wound Care, 18, 98, 10.1097/00129334-200503000-00014 · doi:10.1097/00129334-200503000-00014
  3. Alexiadou, 2012, vol. 3, 4
  4. Sridharan, 2015, Biomaterial based modulation of macrophage polarization: a review and suggested design principles, Mater Today, 18, 313, 10.1016/j.mattod.2015.01.019 · DOI · Paper page
  5. Fang, 2008, A review of becaplermin gel in the treatment of diabetic neuropathic foot ulcers, Biologics, 1
  6. Gilligan, 2018, Cost effectiveness of becaplermin gel on wound closure for the treatment of pressure injuries, Wounds, 30, 197
  7. Bergers, 2005, The role of pericytes in blood-vessel formation and maintenance1, Neuro Oncol, 452, 10.1215/S1152851705000232 · DOI · Paper page
  8. Tuyet, 2009, The efficacy and safety of epidermal growth factor in treatment of diabetic foot ulcers: the preliminary results, Int. Wound J., 6, 159, 10.1111/j.1742-481X.2009.00594.x · doi:10.1111/j.1742-481x.2009.00594.x
  9. Fu, 2000, Recombinant bovine basic fibroblast growth factor accelerates wound healing in patients with burns, donor sites and chronic dermal ulcers, Chin. Med. J., 113, 367
  10. Sakamoto, 2016, Efficacy of gelatin gel sheets in sustaining the release of basic fibroblast growth factor for murine skin defects, J. Surg. Res., 201, 378, 10.1016/j.jss.2015.11.045 · doi:10.1016/j.jss.2015.11.045
  11. Fujita, 2007, Therapeutic angiogenesis induced by controlled release of fibroblast growth factor-2 from injectable chitosan/non-anticoagulant heparin hydrogel in a rat hindlimb ischemia model, Wound Repair Regener, 15, 58, 10.1111/j.1524-475X.2006.00185.x · doi:10.1111/j.1524-475x.2006.00185.x
  12. Zhang, 2009, In situ loading of basic fibroblast growth factor within porous silica nanoparticles for a prolonged release, Nanoscale Res. Lett., 4, 1297, 10.1007/s11671-009-9395-6 · doi:10.1007/s11671-009-9395-6
  13. Losi, 2010, Tissue response to poly(ether)urethane-polydimethylsiloxane-fibrin composite scaffolds for controlled delivery of pro-angiogenic growth factors, Biomaterials, 31, 5336, 10.1016/j.biomaterials.2010.03.033 · doi:10.1016/j.biomaterials.2010.03.033
  14. Hrynyk, 2010, Sustained prolonged topical delivery of bioactive human insulin for potential treatment of cutaneous wounds, Int. J. Pharm., 398, 146, 10.1016/j.ijpharm.2010.07.052 · doi:10.1016/j.ijpharm.2010.07.052
  15. De Luisi, 2013, Erythropoietin is involved in the angiogenic potential of bone marrow macrophages in multiple myeloma, Angiogenesis, 16, 963, 10.1007/s10456-013-9369-2 · doi:10.1007/s10456-013-9369-2
  16. Wen, 2014, Erythropoietin promotes retinal angiogenesis in a mouse model, Mol. Med. Rep., 10, 2979, 10.3892/mmr.2014.2593 · doi:10.3892/mmr.2014.2593
  17. Zhang, 2014, Effects of recombinant human erythropoietin on angiogenesis in chronic ischemic porcine myocardium, Zhonghua wai ke za zhi, 52, 366
  18. Nakamatsu, 2004, Erythropoietin/erythropoietin-receptor system as an angiogenic factor in chemically induced murine hepatic tumors, Int. J. Clin. Oncol., 9, 184, 10.1007/s10147-004-0399-z · doi:10.1007/s10147-004-0399-z
  19. Tang, 2015, A new method of wound treatment: targeted therapy of skin wounds with reactive oxygen species-responsive nanoparticles containing SDF-1alpha, Int. J. Nanomedicine, 10, 6571
  20. Moisenovich, 2015, Novel 3D-microcarriers from recombinant spidroin for regenerative medicine, Dokl. Biochem. Biophys., 463, 232, 10.1134/S1607672915040109 · doi:10.1134/s1607672915040109
  21. Christopher, 2018, Chapter 117 - Vitamin D and critically ill intensive care unit patients, 1177
  22. Wang, 2016, In-situ-generated vasoactive intestinal peptide loaded microspheres in mussel-inspired polycaprolactone nanosheets creating spatiotemporal releasing microenvironment to promote wound healing and angiogenesis, ACS Appl. Mater. Interfaces, 8, 7411, 10.1021/acsami.5b11332 · doi:10.1021/acsami.5b11332
  23. Yang, 2013, Vasoactive intestinal peptide increases VEGF expression to promote proliferation of brain vascular endothelial cells via the cAMP/PKA pathway after ischemic insult in vitro, Peptides, 42, 105, 10.1016/j.peptides.2013.01.007 · doi:10.1016/j.peptides.2013.01.007
  24. Jeon, 2014, The effect of platelet-rich plasma on composite graft survival, Plast. Reconstr. Surg., 134, 239, 10.1097/PRS.0000000000000392 · doi:10.1097/prs.0000000000000392
  25. Kawaguchi, 2014, Effects of liposome-encapsulated hemoglobin on gastric wound healing in the rat, Artif. Organs, 38, 641, 10.1111/aor.12339 · doi:10.1111/aor.12339
  26. Kwok, 2015, Ginsenoside-Rg1 induces angiogenesis by the inverse regulation of MET tyrosine kinase receptor expression through miR-23a, Toxicol. Appl. Pharmacol., 287, 276, 10.1016/j.taap.2015.06.014 · doi:10.1016/j.taap.2015.06.014
  27. Asai, 2012, Topical simvastatin accelerates wound healing in diabetes by enhancing angiogenesis and lymphangiogenesis, Am. J. Pathol., 181, 2217, 10.1016/j.ajpath.2012.08.023 · doi:10.1016/j.ajpath.2012.08.023
  28. Chien, 2010, Intracellular ATP delivery using highly fusogenic liposomes, Methods Mol. Biol., 605, 377, 10.1007/978-1-60327-360-2_26 · doi:10.1007/978-1-60327-360-2_26
  29. Ng, 2014, Carboxymethyl cellulose wafers containing antimicrobials: a modern drug delivery system for wound infections, Eur. J. Pharm. Sci., 51, 173, 10.1016/j.ejps.2013.09.015 · doi:10.1016/j.ejps.2013.09.015
  30. Yasasvini, 2017, Topical hydrogel matrix loaded with Simvastatin microparticles for enhanced wound healing activity, Mater. Sci. Eng. C Mater. Biol. Appl., 72, 160, 10.1016/j.msec.2016.11.038 · doi:10.1016/j.msec.2016.11.038
  31. Biswas, 2003, Plant medicines of Indian origin for wound healing activity: a review, Int J Low Extrem Wounds, 2, 25, 10.1177/1534734603002001006 · doi:10.1177/1534734603002001006
  32. Deed, 1997, Early-response gene signalling is induced by angiogenic oligosaccharides of hyaluronan in endothelial cells. Inhibition by non-angiogenic, high-molecular-weight hyaluronan, Int. J. Cancer, 71, 251, 10.1002/(SICI)1097-0215(19970410)71:2<251::AID-IJC21>3.0.CO;2-J · doi:10.1002/(sici)1097-0215(19970410)71:2<251::aid-ijc21>3.0.co;2-j
  33. Ke, 2015, Co-transplantation of skin-derived precursors and collagen sponge facilitates diabetic wound healing by promoting local vascular regeneration, Cell Physiol Biochem, 37, 1725, 10.1159/000438537 · doi:10.1159/000438537
  34. Zhu, 2016, Overexpression of miR-29b reduces collagen biosynthesis by inhibiting heat shock protein 47 during skin wound healing, Transl. Res., 178, 38, 10.1016/j.trsl.2016.07.001 · DOI
  35. Lucas, 2017, Light-inducible antimiR-92a as a therapeutic strategy to promote skin repair in healing-impaired diabetic mice, Nat. Commun., 8, 10.1038/ncomms15162 · DOI
  36. Ke, 2015, Co-tansplantation of skin-derived precursors and collagen sponge facilitates diabetic wound healing by promoting local vascular regeneration, Cell Physiol Biochem, 37, 1725, 10.1159/000438537 · doi:10.1159/000438537

Cited by

See all 1,021

Metadata

Authors
Veith, A. P., Henderson, K., Spencer, A., Sligar, A. D., & Baker, A. B.
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2019-06
Volume
146
Pages
97-125
ISSN
0169-409X (ISSN-L)
DOI
10.1016/j.addr.2018.09.010
OpenAlex
W2892397780
Cited by
1,021
References
301
FWCI
5.11
Type
journal article
Language
en
Open access
bronze
Licence
Funders
  • American Heart Association (17IRG33410888)
  • DOD CDMRP (W81XWH-16-1-0580, W81XWH-16-1-0582)
  • National Institutes of Health (1R21EB023551-01, 1R21EB024147-01A1, 1R01HL141761-01)
  • NSF (DGE-1610403)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Therapeutic strategies for enhancing angiogenesis in wound healing. https://app.cochat.ai/papers/10.1016/j.addr.2018.09.010
The paper
Veith, A. P., Henderson, K., Spencer, A., Sligar, A. D., & Baker, A. B. (2019). Therapeutic strategies for enhancing angiogenesis in wound healing. Advanced Drug Delivery Reviews. https://doi.org/10.1016/j.addr.2018.09.010

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.